24 results
diagnosis rheumatology treatment algorithm hepatology ards differential disease eosinophilia eosinophils erythematosus gastroenterology hes hypereosinophilia icu lupus sle summary systemic activation
Hypereosinophilia and Hypereosinophilic Syndrome • Secondary Hypereosinophilic Syndrome • Clinically Relevant HES Variants • When to
Hypereosinophilic Syndrome ... • Clinically ... suspect underlying hematologic ... #HES #Hematology ... eosinophils #diagnosis #management
Original ARDSNet Mechanical Ventilation Protocol Acute Respiratory Distress Syndrome Network (ARDSNet) NIH NHLBI ARDS Clinical Network #Management #CriticalCare
Respiratory Distress Syndrome ... NIH NHLBI ARDS Clinical ... Network #Management ... #CriticalCare #
Systemic Lupus Erythematosus - Summary Antinuclear (ANA) - 95% - Initial screening test Anti-dsDNA - 50% • Associated
SLE, including congenital ... block • Sjogren syndrome ... polymyositis overlap syndrome ... Summary #diagnosis #rheumatology ... #management
American College of Critical Care Medicine algorithm for time-sensitive, goal-directed stepwise management of hemodynamic support in
American College of Critical ... goal-directed stepwise management ... 70% (* except congenital ... Shock #Algorithm #CriticalCare ... Pediatrics #Sepsis #Management
Consensus Indications for Irradiated RBC Transfusions: Cellular blood components are irradiated for the prevention of TA-GVHD. Transfused
- Congenital ... disorders (DiGeorge Syndrome ... #Indications #Hematology ... #BloodBank #Management
Acute Respiratory Distress Syndrome – ARDS: Clinical Cheat Sheet An acute diffuse, inflammatory lung injury, leading to
Respiratory Distress Syndrome ... – ARDS: Clinical ... Management ● Early ... RespiratoryDistress #Syndrome ... #CriticalCare
Inherited Non-hemolytic Disorders of Hyperbilirubinemia == Disorders of Conjugation == Gilbert Syndrome: • 5-10% of the population
Conjugation == Gilbert Syndrome ... hyperbilirubinemia syndrome ... as jaundice on clinical ... Hyperbilirubinemia #Inherited #Congenital ... #bilirubin #hepatology
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Constitutional Syndromes ... Aplastic Anemia Clinical ... , Dyskeratosis congenita ... Anemia #oncology #hematology ... #diagnosis #management
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Macrophage Activation Syndrome ... Clinical Presentation ... Fever is the main clinical ... #Diagnosis #Management ... #Hematology #Rheumatology
SAPHO Syndrome Summary What? SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
Rheumatic pain Clinical ... Diagnosis: • A clinical ... #Rheumatology # ... diagnosis #management ... #Dermatology
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